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Alopecia areata may be caused by antibodies targeting specific hair follicle proteins, hindering hair growth.

Hair transplant surgery successfully restored a boy's moustache hair on a cleft lip scar, with natural-looking results and patient satisfaction.

Machine learning can predict how well patients with alopecia areata will respond to certain treatments.

A girl had rickets due to a gene mutation affecting vitamin D response.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The study maps immune changes in mice with alopecia areata to better understand and treat the disease in humans.

The PML protein helps prevent skin cancer in mice.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Certain cytokines may cause or be affected by immune skin diseases, suggesting possible new treatments.

CD44 variant changes start alopecia areata, but don't maintain it.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Murine cytomegalovirus does not cause alopecia areata in these mice.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

Mycophenolate mofetil is a good alternative for autoimmune hepatitis patients who can't tolerate azathioprine.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

Early diagnosis and treatment of hereditary hemochromatosis can prevent serious complications.

The T allele of the PTPN22 gene may increase the risk of alopecia areata.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Poly-L-lactic acid injections can cause hair loss and skin issues.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.